hypercalcaemia Flashcards
what are the commonest causes of hypercalcaemia?
primary hyperparathyroidism, where the parathyroid gland(s) becomes overactive and secretes excess amounts of parathyroid hormone (PTH).
malignancy also
how can you determine the underlying cause for hypercalcaemia?
hallmark of malignancy being the cause is low PTH levels (malignancy is suspected unless proven otherwise),
whereas primary hyperparathyroidism is typically associated with normal or high PTH
what cell type are malignant causes of hypercalcaemia usually associated with?
squamous cell epithelial tumours due to the secretion of PTH related peptide (PTH-rP)
how advanced does a malignancy have to be to be the cause of hypercalcaemia?
occurs in large or advanced tumours
bony mets not always present
other than malignancy, where can hypercalcaemia with low PTH be seen?
in benign granulomatous disease such as TB or sarcoidosis
what does hypercalcaemia with non suppressed PTH suggest?
suggests primary hyperPTH until proven otherwise
what is the most common cause of primary hyperparathyroidism?
a single parathyroid adenoma
parathyroid hyperplasia in more thane gland may suggest a genetic cause
what can a very high serum calcium with a large parathyroid tumour suggest?
parathyroid cancer but this is v rare
may occur rarely in association with jaw tumours (hyperparathyroidism- jaw tumour syndrome)
how high does calcium have to consider hypercalcaemia?
> 2.6 mmol/L
what are the clinical features of hypercalcaemia?
usually asymptomatic and discovered incidentally
non specific symptoms
- tiredness
- generalised aches and pains
specific symptoms
- polyuria
- polydipsia
due to nephrogenic diabetes insipidus
- abdominal pain
- constipation
- psychiatric symptoms
- kidney stones
STONES, MOANS (DEPRESSION), GROANS (ABDO PAIN)
severe metabolic parathyroid bone disease can have a classical cyst appearance on x ray
what will investigations into hypercalcaemia show?
- PTH will be high or non suppressed if primary hyperparathyroidism if the cause
- low phosphate is usually present as PTH causes excretion of phosphate
- High ALP reflects increased bone turnover, common in patients with vit D deficiency
- bone density may be reduced, especially at distal radius
- renal US may show nephrocalcinosis
- sub periosteal erosion of the phalanges may be present in severe disease
what is familial hypocalcinuric hypercalcaemia?
a rare condition caused by a genetic defect in the calcium sensing receptor.
causes abnormally high levels of calcium in the blood (hypercalcemia) and low to moderate levels of calcium in urine (hypocalciuric).
distinguished from primary hyperparathyroidism by showing low urine calcium/creatinine ratio
family history of mild hypercalcaemia
need to exclude FHH before unnecessary next exploration
how is a parathyroid adenoma localised?
hard if lesion is small
parathyroid US will detect usually
SETAMIBI isotope is often used alongside ultrasound
some centres can use SPECT CT / MRI and 4-D CT.
how is hyperparathyroidism treated?
surgery if
- serum calcium is >2.85 mmol/L
- if symptoms debilitating
- if patient is young
parathyroidectomy can be done
medical management where surgery is not desirable or simple observation may be appropriate
Calcimimetic drugs e.g cinacalet are effective at lowering Ca in primary hyperparathyroidism
is acute severe hypercalcaemia a medical emergency?
YES
may present with profound dehydration and renal impairment, requires urgent treatment and consideration of the cause